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Volumn 27, Issue 6, 2002, Pages 477-479
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Dyschromatosis universalis hereditaria
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Author keywords
[No Author keywords available]
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Indexed keywords
MELANIN;
ADULT;
ARTICLE;
CASE REPORT;
CHILD;
CLINICAL OBSERVATION;
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA;
DYSTROPHY;
FEMALE;
FOOT SOLE;
HAND PALM;
HISTOPATHOLOGIC SKIN REACTION;
HUMAN;
HUMAN TISSUE;
HYPERPIGMENTATION;
HYPOPIGMENTATION;
INDIAN;
MALE;
MELANOSOME;
MOUTH MUCOSA;
NAIL DISEASE;
PATHOGENESIS;
PIGMENT DISORDER;
PRIORITY JOURNAL;
PTERYGIUM;
SKIN DISEASE;
TONGUE;
ADOLESCENT;
CHILD;
FEMALE;
HUMANS;
MALE;
MOUTH DISEASES;
PIGMENTATION DISORDERS;
SKIN DISEASES, GENETIC;
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EID: 0036413571
PISSN: 03076938
EISSN: None
Source Type: Journal
DOI: 10.1046/j.1365-2230.2002.01129.x Document Type: Article |
Times cited : (35)
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References (10)
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